165 research outputs found

    Childhood body-mass index and the risk of coronary heart disease in adulthood

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    BACKGROUND: The worldwide epidemic of childhood obesity is progressing at an alarming rate. Risk factors for coronary heart disease (CHD) are already identifiable in overweight children. The severity of the long-term effects of excess childhood weight on CHD, however, remains unknown. METHODS: We investigated the association between body-mass index (BMI) in childhood (7 through 13 years of age) and CHD in adulthood (25 years of age or older), with and without adjustment for birth weight. The subjects were a cohort of 276,835 Danish schoolchildren for whom measurements of height and weight were available. CHD events were ascertained by linkage to national registers. Cox regression analyses were performed. RESULTS: In 5,063,622 person-years of follow-up, 10,235 men and 4318 women for whom childhood BMI data were available received a diagnosis of CHD or died of CHD as adults. The risk of any CHD event, a nonfatal event, and a fatal event among adults was positively associated with BMI at 7 to 13 years of age for boys and 10 to 13 years of age for girls. The associations were linear for each age, and the risk increased across the entire BMI distribution. Furthermore, the risk increased as the age of the child increased. Adjustment for birth weight strengthened the results. CONCLUSIONS: Higher BMI during childhood is associated with an increased risk of CHD in adulthood. The associations are stronger in boys than in girls and increase with the age of the child in both sexes. Our findings suggest that as children are becoming heavier worldwide, greater numbers of them are at risk of having CHD in adulthood

    Changing consumption of resources for respiratory support and short-term outcomes in four consecutive geographical cohorts of infants born extremely preterm over 25 years since the early 1990s

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    OBJECTIVES:It is unclear how newer methods of respiratory support for infants born extremely preterm (EP; 22-27 weeks gestation) have affected in-hospital sequelae. We aimed to determine changes in respiratory support, survival and morbidity in EP infants since the early 1990s. DESIGN:Prospective longitudinal cohort study. SETTING:The State of Victoria, Australia. PARTICIPANTS:All EP births offered intensive care in four discrete eras (1991-1992 (24 months): n=332, 1997 (12 months): n=190, 2005 (12 months): n=229, and April 2016-March 2017 (12 months): n=250). OUTCOME MEASURES:Consumption of respiratory support, survival and morbidity to discharge home. Cost-effectiveness ratios describing the average additional days of respiratory support associated per additional survivor were calculated. RESULTS:Median duration of any respiratory support increased from 22 days (1991-1992) to 66 days (2016-2017). The increase occurred in non-invasive respiratory support (2 days (1991-1992) to 51 days (2016-2017)), with high-flow nasal cannulae, unavailable in earlier cohorts, comprising almost one-half of the duration in 2016-2017. Survival to discharge home increased (68% (1991-1992) to 87% (2016-2017)). Cystic periventricular leukomalacia decreased (6.3% (1991-1992) to 1.2% (2016-2017)), whereas retinopathy of prematurity requiring treatment increased (4.0% (1991-1992) to 10.0% (2016-2017)). The average additional costs associated with one additional infant surviving in 2016-2017 were 200 (95% CI 150 to 297) days, 326 (183 to 1127) days and 130 (70 to 267) days compared with 1991-1992, 1997 and 2005, respectively. CONCLUSIONS:Consumption of resources for respiratory support has escalated with improved survival over time. Cystic periventricular leukomalacia reduced in incidence but retinopathy of prematurity requiring treatment increased. How these changes translate into long-term respiratory or neurological function remains to be determined.Jeanie L Y Cheong, Joy E Olsen, Li Huang, Kim M Dalziel, Rosemarie A Boland, Alice C Burnett ... et al

    Measurements of the Mass and Full-Width of the ηc\eta_c Meson

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    In a sample of 58 million J/ψJ/\psi events collected with the BES II detector, the process J/ψ→γηc\psi\to\gamma\eta_c is observed in five different decay channels: γK+K−π+π−\gamma K^+K^-\pi^+\pi^-, γπ+π−π+π−\gamma\pi^+\pi^-\pi^+\pi^-, γK±KS0π∓\gamma K^\pm K^0_S \pi^\mp (with KS0→π+π−K^0_S\to\pi^+\pi^-), γϕϕ\gamma \phi\phi (with ϕ→K+K−\phi\to K^+K^-) and γppˉ\gamma p\bar{p}. From a combined fit of all five channels, we determine the mass and full-width of ηc\eta_c to be mηc=2977.5±1.0(stat.)±1.2(syst.)m_{\eta_c}=2977.5\pm1.0 ({stat.})\pm1.2 ({syst.}) MeV/c2c^2 and Γηc=17.0±3.7(stat.)±7.4(syst.)\Gamma_{\eta_c} = 17.0\pm3.7 ({stat.})\pm7.4 ({syst.}) MeV/c2c^2.Comment: 9 pages, 2 figures and 4 table. Submitted to Phys. Lett.

    Size Doesn't Matter: Towards a More Inclusive Philosophy of Biology

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    notes: As the primary author, O’Malley drafted the paper, and gathered and analysed data (scientific papers and talks). Conceptual analysis was conducted by both authors.publication-status: Publishedtypes: ArticlePhilosophers of biology, along with everyone else, generally perceive life to fall into two broad categories, the microbes and macrobes, and then pay most of their attention to the latter. ‘Macrobe’ is the word we propose for larger life forms, and we use it as part of an argument for microbial equality. We suggest that taking more notice of microbes – the dominant life form on the planet, both now and throughout evolutionary history – will transform some of the philosophy of biology’s standard ideas on ontology, evolution, taxonomy and biodiversity. We set out a number of recent developments in microbiology – including biofilm formation, chemotaxis, quorum sensing and gene transfer – that highlight microbial capacities for cooperation and communication and break down conventional thinking that microbes are solely or primarily single-celled organisms. These insights also bring new perspectives to the levels of selection debate, as well as to discussions of the evolution and nature of multicellularity, and to neo-Darwinian understandings of evolutionary mechanisms. We show how these revisions lead to further complications for microbial classification and the philosophies of systematics and biodiversity. Incorporating microbial insights into the philosophy of biology will challenge many of its assumptions, but also give greater scope and depth to its investigations

    Measurement of Branching Ratios for ηc\eta_c Hadronic Decays

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    In a sample of 58 million J/ψJ/\psi events collected with the BES II detector, the process J/ψ→γηc\psi\to\gamma\eta_c is observed in five decay channels: ηc→K+K−π+π−\eta_c \to K^+K^-\pi^+\pi^-, π+π−π+π−\pi^+\pi^-\pi^+\pi^-, K±KS0π∓K^\pm K^0_S \pi^\mp (with KS0→π+π−K^0_S\to\pi^+\pi^-), ϕϕ\phi\phi (with ϕ→K+K−\phi\to K^+K^-) and ppˉp\bar{p}. From these signals, we determine Br(J/ψ→γηc)×Br(ηc→K+K−π+π−)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to K^+K^-\pi^+\pi^-) =(1.5±0.2±0.2)×10−4=(1.5\pm0.2\pm0.2)\times10^{-4}, Br(J/ψ→γηc)×Br(ηc→π+π−π+π−)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to \pi^+\pi^-\pi^+\pi^-) =(1.3±0.2±0.4)×10−4=(1.3\pm0.2\pm0.4)\times10^{-4}, Br(J/ψ→γηc)×Br(ηc→K±KS0π∓)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to K^\pm K_{S}^{0}\pi^\mp) =(2.2±0.3±0.5)×10−4=(2.2\pm0.3\pm0.5)\times10^{-4}, Br(J/ψ→γηc)×Br(ηc→ϕϕ)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to \phi\phi) =(3.3±0.6±0.6)×10−5=(3.3\pm0.6\pm0.6)\times10^{-5} and Br(J/ψ→γηc)×Br(ηc→ppˉ)Br(J/\psi\to\gamma\eta_c)\times Br(\eta_c\to p\bar{p}) =(1.9±0.3±0.3)×10−5=(1.9\pm0.3\pm0.3)\times10^{-5}.Comment: 8 pages, 1 figures and 4 table. Submitted to Phys. Lett.

    Evidence of psi(3770) non-DD-bar Decay to J/psi pi+pi-

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    Evidence of ψ(3770)\psi(3770) decays to a non-DDˉ{D \bar D} final state is observed. A total of 11.8±4.8±1.311.8 \pm 4.8 \pm 1.3 \psi(3770) \to \PPJP events are obtained from a data sample of 27.7 pb−1\rm {pb^{-1}} taken at center-of-mass energies around 3.773 GeV using the BES-II detector at the BEPC. The branching fraction is determined to be BF(\psi(3770) \to \PPJP)=(0.34\pm 0.14 \pm 0.09)%, corresponding to the partial width of \Gamma(\psi(3770) \to \PPJP) = (80 \pm 33 \pm 23) keV.Comment: 8 pages, 7 figures, Submitted to Physics Letters

    Measurements of J/psi --> p \bar{p}

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    The process J/\psi --> p \bar{p} is studied using 57.7 X 10^6 J/\psi events collected with the BESII detector at the Beijing Electron Positron Collider. The branching ratio is determined to be Br(J/\psi --> p \bar{p})=(2.26 +- 0.01 +- 0.14) X 10^{-3}, and the angular distribution is well described by \frac{dN}{d cos\theta_p}=1+\alpha\cos^2\theta_p with \alpha = 0.676 +- 0.036 +- 0.042, where \theta_p is the angle between the proton and beam directions. The value of \alpha obtained is in good agreement with the predictions of first-order QCD.Comment: 6 pages, 2 figures, RevTex4, Submitted to Phys.Lett.

    Search for K_S K_S in J/psi and psi(2S) decays

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    The CP violating processes J/psi-->K_S K_S and psi(2S)-->K_S K_S are searched for using samples of 58 million J/psi and 14 million psi(2S) events collected with the Beijing Spectrometer at the Beijing Electron Positron Collider. No signal is observed, and upper limits on the decay branching ratios are determined to be BR(J/psi-->K_S K_S) K_S K_S) < 4.6x10^{-6} at the 95% confidence level.Comment: 6 pages, 4 figures, submitted to Phys. Lett.
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